NUBPL mitochondrial disease: new patients and review of the genetic and clinical spectrum

Kimonis, V. et al. (2021) NUBPL mitochondrial disease: new patients and review of the genetic and clinical spectrum. Journal of Medical Genetics, 58(5), pp. 314-325. (doi: 10.1136/jmedgenet-2020-106846) (PMID:32518176)

[img] Text
217961.pdf - Accepted Version
Available under License Creative Commons Attribution Non-commercial.

718kB

Abstract

Background: The nucleotide binding protein-like (NUBPL) gene was first reported as a cause of mitochondrial complex I deficiency (MIM 613621, 618242) in 2010. To date, only eight patients have been reported with this mitochondrial disorder. Five other patients were recently reported to have NUBPL disease but their clinical picture was different from the first eight patients. Here, we report clinical and genetic findings in five additional patients (four families). Methods: Whole exome sequencing was used to identify patients with compound heterozygous NUBPL variants. Functional studies included RNA-Seq transcript analyses, missense variant biochemical analyses in a yeast model (Yarrowia lipolytica) and mitochondrial respiration experiments on patient fibroblasts. Results: The previously reported c.815-27T>C branch-site mutation was found in all four families. In prior patients, c.166G>A [p.G56R] was always found in cis with c.815-27T>C, but only two of four families had both variants. The second variant found in trans with c.815-27T>C in each family was: c.311T>C [p.L104P] in three patients, c.693+1G>A in one patient and c.545T>C [p.V182A] in one patient. Complex I function in the yeast model was impacted by p.L104P but not p.V182A. Clinical features include onset of neurological symptoms at 3–18 months, global developmental delay, cerebellar dysfunction (including ataxia, dysarthria, nystagmus and tremor) and spasticity. Brain MRI showed cerebellar atrophy. Mitochondrial function studies on patient fibroblasts showed significantly reduced spare respiratory capacity. Conclusion: We report on five new patients with NUBPL disease, adding to the number and phenotypic variability of patients diagnosed worldwide, and review prior reported patients with pathogenic NUBPL variants.

Item Type:Articles
Additional Information:Funding for these studies were provided by the Spooner Girls Foundation, CART (Center for Autism Research and Translation) and the ICTS (Institute of Clinical Translational Science, UC Irvine).
Keywords:Neurogenetics, clinical genetics, metabolic disorders, molecular genetics, neurology.
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:MacLean, Dr Andrew
Authors: Kimonis, V., al Dubaisi, R., Maclean, A. E., Hall, K., Weiss, L., Stover, A. E., Schwartz, P. H., Berg, B., Cheng, C., Parikh, S., Conner, B. R., Wu, S., Hasso, A. N., Scott, D. A., Koenig, M. K., Karam, R., Tang, S., Smith, M., Chao, E., Balk, J., Hatchwell, E., and Eis, P. S.
College/School:College of Medical Veterinary and Life Sciences > Institute of Infection Immunity and Inflammation
Journal Name:Journal of Medical Genetics
Publisher:BMJ Publishing Group
ISSN:0022-2593
ISSN (Online):1468-6244
Published Online:09 June 2020
Copyright Holders:Copyright © 2020 The Authors
First Published:First published in Journal of Medical Genetics 58(5): 314-325
Publisher Policy:Reproduced in accordance with the publisher copyright policy

University Staff: Request a correction | Enlighten Editors: Update this record